T-URF13 Protein from Mitochondria of Texas Male-Sterile Maize (Zea mays L.)

Thumbnail Image
Date
1991-03-01
Authors
Hack, Ethan
Lin, Chentao
Yang, Hongyun
Horner, Harry
Major Professor
Advisor
Committee Member
Journal Title
Journal ISSN
Volume Title
Publisher
Authors
Person
Horner, Harry
University Professor Emeritus
Research Projects
Organizational Units
Organizational Unit
Botany
The Botany Graduate Program offers work for the degrees Master of Science and Doctor of Philosophy with a graduate major in Botany, and minor work for students majoring in other departments or graduate programs. Within the Botany Graduate Major, one of the following areas of specialization may be designated: aquatic and wetland ecology, cytology, ecology, morphology, mycology, physiology and molecular biology, or systematics and evolution. Relevant graduate courses that may be counted toward completion of these degrees are offered by the Departments of EEOB and GDCB, and by other departments and programs. The specific requirements for each student’s course distribution and research activities are set by the Program of Study Committee established for each student individually, and must satisfy all requirements of the Graduate College (See Index). GRE (and if necessary, TOEFL) scores are required of all applicants; students are encouraged to contact faculty prior to application.
Journal Issue
Is Version Of
Versions
Series
Department
Botany
Abstract

The protein T-URF13 (URF13) is specific to mitochondria of maize (Zea mays L.) with Texas (T) male-sterile cytoplasm and has been implicated in causing male sterility and susceptibility to T-cytoplasm-specific fungal diseases. T-URF13 was purified from isolated mitochondria from maize (line B73) with T cytoplasm by gel filtration and a quasi two-dimensional polyacrylamide gel electrophoresis system. Antibodies to the purified and denatured protein were produced in rabbits. Anti-T-URF13 antiserum was used to show that T-URF13 is in the inner membrane of mitochondria and behaves as an integral membrane protein when mitochondria are fractionated with sodium carbonate or Triton X-114. The antiserum and protein A tagged with 20-nanometer-gold particles were used to localize T-URF13 in T mitochondria by electron microscopy of sections of isolated mitochondria from etiolated shoots and sections of roots and of tapetal cells at pre-and post-degeneration stages of microsporogenesis. The microscopic study confirms that T-URF13 is specifically localized in the mitochondrial membranes of all of the T mitochondria tested, notably those in the tapetum from the meiocyte stage to the late-microspore stage. No change in the amount of labeled T-URF13 protein in the mitochondria of aging tapetal cells was detected.

Comments

This aritcle is published as Hack, Ethan, Chentao Lin, Hongyun Yang, and Harry T. Horner. "T-URF 13 protein from mitochondria of Texas male-sterile maize (Zea mays L.): Its purification and submitochondrial localization, and immunogold labeling in anther tapetum during microsporogenesis." Plant physiology 95, no. 3 (1991): 861-870. doi: 10.1104/pp.95.3.861. Copyright American Society of Plant Biologists. Posted with pemission.

Description
Keywords
Citation
DOI
Copyright
Tue Jan 01 00:00:00 UTC 1991
Collections